VCD Analysis of Axial Chirality in Synthetic Stereoisomeric Biaryl-Type bis-Isochroman Heterodimers with Isolated Blocks of Central and Axial Chirality

Optically active heterodimeric 5,5′-linked bis-isochromans, containing a stereogenic ortho-trisubstituted biaryl axis and up to four chirality centers, were synthesized stereoselectively by using a Suzuki–Miyaura biaryl coupling reaction of optically active isochroman and 1-arylpropan-2-ol derivatives, providing the first access to synthetic biaryl-type isochroman dimers. Enantiomeric pairs and stereoisomers up to seven derivatives were prepared with four different substitution patterns, which enabled us to test how OR, ECD, and VCD measurements and DFT calculations can be used to determine parallel central and axial chirality elements in three isolated blocks of chirality. In contrast to natural penicisteckins A–D and related biaryls, the ECD spectra and OR data of (aS) and (aR) atropodiastereomers did not reflect the opposite axial chirality, but they were characteristic of the central chirality. The atropodiastereomers showed consistently near-mirror-image VCD curves, allowing the determination of axial chirality with the aid of DFT calculation or by comparison of characteristic VCD transitions.

Benzene-condensed chiral O-heterocycles often form biaryl-type homo-or heterodimeric natural products with a stereogenic biaryl axis, the formation of which is aided by the presence of activating substituents of the benzene ring such as hydroxyl or alkoxy groups [7].Depending on the substitution pattern, the hindered rotation along the biaryl axis can result in atropisomers with axial chirality [7] or interconverting conformers with different biaryl helicity [8].The axial chirality of biaryls is mainly governed by the number and size of the ortho-substituents, which impose strong steric repulsion in the periplanar transition state, and, thus, hinder the rotation about the biaryl axis.The axial chirality of biaryl natural products often plays a fundamental role in the bioactivity, since atropodiastereomers can possess markedly different activity [9][10][11][12][13].
Although chiral isochroman natural products often contain activating hydroxyl or alkoxy groups on the condensed benzene ring, which would promote oxidative biaryl coupling reactions, there are only two reports on biaryl-type bis-isochroman natural products produced by oxidative biaryl coupling [14,15].The homodimeric 7,7 ′ -linked asperbiphenyl (1), the first axially chiral bis-isochroman, was isolated from the marine fungus Aspergillus sp. and it contains an ortho-tetrasubstituted stereogenic biaryl axis and four chirality centers [14].
The absolute configurations of penicisteckins A-D (2-5) were determined by singlecrystal X-ray diffraction analysis, while those of penicisteckin E (6) and F (7) by TDDFT (time-dependent density functional theory)-ECD calculations of the atropodiastereomers [15].The configurational assignment of both central and axial stereogenic elements in biaryl natural products is still a challenging task when single-crystal X-ray analysis and chemical correlation is not applicable.In this case, the combination of electronic (ECD) and vibrational circular dichroism (VCD), and optical rotation (OR) calculations may offer a solution.Biaryltype atropodiastereomers usually have near-mirror-image ECD spectra when their biaryl chromophore is not symmetrical [16], which can be used for the assignment of axial chirality with the aid of TDDFT-ECD calculations [17][18][19].
The sign and magnitude of the biaryl dihedral angle of the two aryl units in axially chiral biaryls are reflected in the interaction of the two aromatic chromophores, giving rise to exciton-coupled ECD bands.The signs of the exciton-coupled ECD couplets are usually characteristic of the axial chirality, as exemplified by the mirror-image ECD spectra of flavomannin A and B, atropodiastereomeric dihydroanthracenone dimers [20].However, ECD data do not reflect the absolute configuration of the central chirality elements when they are also present in the condensed heterocyclic rings of biaryls.When the optically active monomeric units are also coisolated with the dimers, they can be analyzed independently by chiroptical methods to assign the central chirality [16][17][18][19][20][21].The central and axial chirality elements of cephalochromin, a homodimeric naphthpyranone natural product, could be determined simultaneously by VCD calculations [22], but the same approach failed to determine the central chirality elements of flavomannin A [20].Recently, the axial chirality of 9,10-phenanthrenequinone dimers has been determined by ECD calculations, while the central chirality of the side chains were assigned by TDDFT-OR calculations [23].
In the current work, we carried out the synthesis of optically active 5,5 ′ -linked bisisochromans with known absolute configuration and different substitution pattern at C-1 and C-1 ′ , which contain an ortho-trisubstituted stereogenic biaryl axis and up to four chirality centers (Scheme 1).This is the first synthesis of the bis-isochroman scaffold with central and axial chirality.
The stereoselective synthesis enabled us to change the absolute configurations of both axial and central chirality elements and to prepare up to seven stereoisomeric products, including enantiomeric pairs and atropodiastereomers.The stereogenic elements constituted three isolated blocks of chirality, which consisted of the axial chirality and central chirality elements of the two isochroman subunits.The correlation of the configuration for these blocks of chirality is a very common and significant challenge in the stereochemical assignment of axially chiral biaryl-type homo-and heterodimers containing benzene-condensed heterocycles as monomeric units.The stereoisomeric bis-isochromans served as model compounds to test the combination of ECD, VCD, and OR measurements and calculations to determine the parallel axial and central chirality elements.With the stereoisomeric The stereoselective synthesis enabled us to change the absolute configurations of both axial and central chirality elements and to prepare up to seven stereoisomeric products, including enantiomeric pairs and atropodiastereomers.The stereogenic elements constituted three isolated blocks of chirality, which consisted of the axial chirality and central chirality elements of the two isochroman subunits.The correlation of the configuration for these blocks of chirality is a very common and significant challenge in the stereochemical assignment of axially chiral biaryl-type homo-and heterodimers containing benzene-condensed heterocycles as monomeric units.The stereoisomeric bis-isochromans served as model compounds to test the combination of ECD, VCD, and OR measurements and calculations to determine the parallel axial and central chirality elements.With the stereoisomeric bis-isochromans in hand, we could test how the different methods could Scheme 1. Retrosynthetic scheme for the preparation of axially chiral heterodimeric bis-ischromans.
In addition to the chiroptical approach, the combination of NOE correlations and DFT conformational analysis was also tested to correlate the relative configuration of axial and central chirality elements.The planar structure and absolute configuration were confirmed independently by single-crystal X-ray analysis for three bis-isochroman derivatives.
According to our retrosynthetic plan, the target bis-isochromans A were obtained by an oxa-Pictet-Spengler cyclization reaction of the axially chiral isochroman/1-arylpropan- During the synthesis of the target bis-isochromans A, we could change the absolute configuration of the C-3 and C-3 ′ chirality centers by using (R)-propylene oxide [(R)-11] [29] instead of (S)-11, which allowed the preparation of enantiomeric pairs.The formation of new axial and central chirality stereogenic elements during the biaryl cross-coupling and oxa-Pictet-Spengler reactions produced a series of stereoisomeric bis-isochromans, which were analyzed by ECD, VCD, OR, NOE measurements, X-ray analysis, and DFT calculations.
and central chirality elements.The planar structure and absolute configuration were confirmed independently by single-crystal X-ray analysis for three bis-isochroman derivatives.
According to our retrosynthetic plan, the target bis-isochromans A were obtained by an oxa-Pictet-Spengler cyclization reaction of the axially chiral isochroman/1-arylpropan-2-ol conjugate B, which diastereoselectively established a new C-1′ chirality center and allowed the variation of the C-1 substituent (Scheme 1).The key step of the scheme is the Suzuki-Miyaura biaryl cross-coupling reaction of cis-or trans-5-iodoisochromans C with the pinacolatoboronate ester derivative (S)-8, which produced the ortho-trisubstituted stereogenic biaryl axis [C + (S)-8 → B].Chirality transfer from central to axial is expected to take place during formation of the biaryl axis.The boronate ester derivative (S)-8 and the 5-iodoisochromans C could be traced back to (S)-propylenoxide [(S)-11] [28] in two separate three-and four-step sequences.
During the synthesis of the target bis-isochromans A, we could change the absolute configuration of the C-3 and C-3′ chirality centers by using (R)-propylene oxide [(R) -11] [29] instead of (S)-11, which allowed the preparation of enantiomeric pairs.The formation of new axial and central chirality stereogenic elements during the biaryl cross-coupling and oxa-Pictet-Spengler reactions produced a series of stereoisomeric bis-isochromans, which were analyzed by ECD, VCD, OR, NOE measurements, X-ray analysis, and DFT calculations.

Stereochemical Analysis
Seven stereoisomers of 21, containing three known chirality centers along with the stereogenic biaryl axis, were used as model compounds for ECD, VCD, and OR measurements and calculations to test how to determine the axial chirality in the presence of central chirality elements or vice versa.Six stereoisomers of both 22 and 23, consisting of three enantiomeric pairs, were prepared for the stereochemical analysis, which contained four known chirality centers along with the stereogenic biaryl axis.We studied two atropodiastereomers of 28, which had only two central chirality elements with the same (S) absolute configuration.
The enantiomeric pairs of 21-23 provided mirror-image experimental ECD and VCD curves, which allowed the validation of the weak Cotton effects (CEs) and artefacts as well as our VCD measurement protocol (Figures S153-158, S173-178, S185-190).Experimental and computed ECD, VCD, and OR data of atropodiastereomers of 21 were compared to identify chiroptical features that can deduce the axial chirality in the presence of central chirality elements.Surprisingly, the atropodiastereomeric cis-(aR,1R,3S,3 ′ S)and cis-(aS,1R,3S,3 ′ S)-21 showed near-identical ECD spectra with a broad negative couplet below 300 nm (Figure 1a), which were not suitable to distinguish the atropodiastereomers and assign the axial chirality.The experimental ECD curves of cis-(aR,1R,3S,3 ′ S)and cis-(aS,1R,3S,3 ′ S)-21 differed only in the intensities and they were reproduced well by the corresponding computed B3LYP/TZVP PCM/MeCN ECD spectra.In axially chiral biaryl natural products, the sign and magnitude of the biaryl dihedral angle usually primarily governs the exciton-coupled ECD spectrum, the pattern of which is characteristic of the axial chirality even in the presence of central chirality elements.The anomalous ECD behavior of the atropodiastereomeric cis-(aR,1R,3S,3 ′ S)and cis-(aS,1R,3S,3 ′ S)-21 could be attributed to either the presence of the C-1 4-fluorophenyl group, which could interact with the biaryl chromophore with exciton coupling, or the substitution pattern of the 5,5 ′ -linked biaryl, which provided near parallel orientation of the interacting electric transition moments of the two isochroman subunits.In contrast, the experimental VCD spectra of cis-(aR,1R,3S,3 ′ S)and cis-(aS,1R,3S,3 ′ S)-21 showed almost mirror-image curves in the wavenumber range 1100-1450 cm −1 , which reflected the different axial chirality of the atropodiastereomers, and they could be reproduced well by the VCD calculations (Figure 1b).On the basis of the good agreements, the axial chirality could be assigned to the near-mirror-image VCD curves.astereomers of 28, which had only two central chirality elements with the same (S) absolute configuration.
The enantiomeric pairs of 21-23 provided mirror-image experimental ECD and VCD curves, which allowed the validation of the weak Cotton effects (CEs) and artefacts as well as our VCD measurement protocol (Figures S153-158, S173-178, S185-190).Experimental and computed ECD, VCD, and OR data of atropodiastereomers of 21 were compared to identify chiroptical features that can deduce the axial chirality in the presence of central chirality elements.Surprisingly, the atropodiastereomeric cis-(aR,1R,3S,3′S)-and cis-(aS,1R,3S,3′S)-21 showed near-identical ECD spectra with a broad negative couplet below 300 nm (Figure 1a), which were not suitable to distinguish the atropodiastereomers and assign the axial chirality.The experimental ECD curves of cis-(aR,1R,3S,3′S)-and cis-(aS,1R,3S,3′S)-21 differed only in the intensities and they were reproduced well by the corresponding computed B3LYP/TZVP PCM/MeCN ECD spectra.In axially chiral biaryl natural products, the sign and magnitude of the biaryl dihedral angle usually primarily governs the exciton-coupled ECD spectrum, the pattern of which is characteristic of the axial chirality even in the presence of central chirality elements.The anomalous ECD behavior of the atropodiastereomeric cis-(aR,1R,3S,3′S)-and cis-(aS,1R,3S,3′S)-21 could be attributed to either the presence of the C-1 4-fluorophenyl group, which could interact with the biaryl chromophore with exciton coupling, or the substitution pattern of the 5,5′linked biaryl, which provided near parallel orientation of the interacting electric transition moments of the two isochroman subunits.In contrast, the experimental VCD spectra of cis-(aR,1R,3S,3′S)-and cis-(aS,1R,3S,3′S)-21 showed almost mirror-image curves in the wavenumber range 1100-1450 cm −1 , which reflected the different axial chirality of the atropodiastereomers, and they could be reproduced well by the VCD calculations (Figure 1b).On the basis of the good agreements, the axial chirality could be assigned to the nearmirror-image VCD curves.The ECD spectra of the atropodiastereomeric trans-(aR,1R,3S,3 ′ S)and trans-(aS,1R,3S,3 ′ S)-21 also had quite a similar pattern; they had a negative CE around 240 nm and a more intense positive one below 210 nm (Figure 2a).The weak negative CE at 215 nm of trans-(aS,1S,3S,3 ′ S)-21 represented the sole slight difference that could be reproduced well by the ECD calculations to differentiate the (aS) and (aR) atropodiastereomers.However, the experimental ECD spectra of both atropodiastereomers and enantiomers were required for this assignment, and if only one of the two atropodiastereomers was available for ECD measurement, a reliable assignment of the axial chirality could not be achieved by the ECD calculations.There were much more apparent differences in the experimental VCD spectra of trans-(aR,1R,3S,3 ′ S)and trans-(aS,1R,3S,3 ′ S)-21, since near-mirror-image VCD transitions were recorded in the range of 1050-1450 cm −1 (Figure 2b).The VCD transitions were clearly determined by the opposite axial chirality, which were reproduced well by the DFT VCD calculations.The agreement of the experimental and computed VCD spectra was utilized to determine the axial chirality.and a more intense positive one below 210 nm (Figure 2a).The weak negative CE at 215 nm of trans-(aS,1S,3S,3′S)-21 represented the sole slight difference that could be reproduced well by the ECD calculations to differentiate the (aS) and (aR) atropodiastereomers.However, the experimental ECD spectra of both atropodiastereomers and enantiomers were required for this assignment, and if only one of the two atropodiastereomers was available for ECD measurement, a reliable assignment of the axial chirality could not be achieved by the ECD calculations.There were much more apparent differences in the experimental VCD spectra of trans-(aR,1R,3S,3′S)-and trans-(aS,1R,3S,3′S)-21, since nearmirror-image VCD transitions were recorded in the range of 1050-1450 cm −1 (Figure 2b).The VCD transitions were clearly determined by the opposite axial chirality, which were reproduced well by the DFT VCD calculations.The agreement of the experimental and computed VCD spectra was utilized to determine the axial chirality.The OR values of the four stereoisomers cis-(aR/aS,1R,3S,3 ′ S)and trans-(aR/aS,1S,3S,3 ′ S)-21 were recorded in acetonitrile at 589, 578, 546, 436, and 365 nm and computed with the BH&HLYP/TZVP PCM/MeCN method (Figure 2c).
Both atropodiastereomers cis-(aR/aS,1R,3S,3 ′ S)-21 gave monotonously increasing positive ORD curves in the 589-365 nm wavelength range, with cis-(aR,1R,3S,3 ′ S)-21 giving significantly larger magnitudes, which could be reproduced well by the OR calculations.The reproduction of the differences in the intensity of the positive OR values of cis-(aR/aS,1R,3S,3 ′ S)-21 by OR calculations may be used to assign the (aR)/(aS) axial chirality.However, this approach would be only feasible when the experimental OR values of both atropodiastereomers are available, which is usually not the case.The two atropodiastereomers trans-(aR/aS,1S,3S,3 ′ S)-21 showed a monotonously decreasing ORD curve with the same negative signs but different intensities.The ORD curve of trans-(aR,1S,3S,3 ′ S)-21 ran above that of trans-(aS,1S,3S,3 ′ S)-21, and were reproduced well by the OR calculations.The OR values recorded at five wavelengths showed identical positive and negative signs for the atropodiastereomeric pairs cis-(aR/aS,1R,3S,3 ′ S)and trans-(aR/aS,1S,3S,3 ′ S)-21, respectively.Although there were consistent differences in the magnitudes, they could not be used to distinguish and assign the atropodiastereomers efficiently.In contrast, the C-1 epimeric pairs cis-(aR,1R,3S,3 ′ S)/trans-(aR,1S,3S,3 ′ S)-21 and cis-(aS,1R,3S,3 ′ S)/trans-(aS,1S,3S,3 ′ S)-21 differing only in the absolute configuration of the C-1 chirality center had oppositely signed OR values at all the tested wavelengths, which could be used to assign the AC of C-1.
The comparison of the experimental ECD of the four stereoisomers cis-(aR/aS,1R,3S,3 ′ S)and trans-(aR/aS,1S,3S,3 ′ S)-21 showed that there are significant differences in the sign, shape, and intensity of the ECD bands for the C-1 epimeric pairs cis-(aR,1R,3S,3 ′ S)/trans-(aR,1S,3S,3 ′ S)-21 and cis-(aS,1R,3S,3 ′ S)/trans-(aS,1S,3S,3 ′ S)-21 in the wavelength range 210-230 nm (Figure 3a).For instance, the cis-(aS,1R,3S,3 ′ S)-21 had an intense negative CE at 224 nm, while the epimeric trans-(aS,1S,3S,3 ′ S)-21 showed a weak positive CE at 221 nm and a weak negative one at 215 nm.Similarly, the cis-(aR,1R,3S,3 ′ S)-21 exhibited an intense negative CE at 226 nm, while the epimeric trans-(aR,1S,3S,3 ′ S)-21 had a positive shoulder at that wavelength.When aided with TDDFT-ECD calculations, the ECD spectra could distinguish and assign efficiently the C-1 epimers of 21 but they cannot be used to determine the axial chirality.C-1 epimers had significant differences in the 220-240 nm range, while minor differences appeared for the weak C-H deformation vibrations (1200-1300 cm −1 ) in the VCD spectra.In contrast, the VCD spectra of the four stereoisomers cis-(aR/aS,1R,3S,3 ′ S)and trans-(aR/aS,1S,3S,3 ′ S)-21 showed near-mirror-image VCD transitions for the (aR)/(aS) atropodiastereomeric pairs allowing the assignment of the axial chirality with the aid of DFT VCD calculations (Figure 3b).Regarding the C-1 epimeric pairs cis-(aR,1R,3S,3 ′ S)/trans-(aR,1S,3S,3 ′ S)-21 and cis-(aS,1R,3S,3 ′ S)/trans-(aS,1S,3S,3 ′ S)-21, the VCD showed only minor differences in weak transitions in the range of 1250-1270 cm −1 .When considering diastereomeric pairs differing in the absolute configuration of one, two, or three chirality centers but having identical axial chirality, the ECD spectra were markedly different or near mir-ror image (Figure S163), while the VCD spectra showed no or only minor differences, especially in the 1200-1300 cm −1 wavenumber range (Figures S161-S172).For instance, stereoisomers differing in all the three chirality centers such as trans-(aR,1S,3S,3 ′ S)-21 and trans-(aR,1R,3R,3 ′ R)-21 had quite different ECD curves with opposite CE below 220 nm, while the main VCD transitions had the same signs and only small differences could be observed in the range of 1200-1300 cm −1 (Figure 4).Similarly, stereoisomers differing in the C-3 and C-3 ′ chirality centers such as trans-(aR,1S,3S,3 ′ S)-21 and cis-(aR,1S,3R,3 ′ R)-21 showed opposite CEs in the ECD spectra below 220 nm, while minor VCD differences were again restricted to the range of 1200-1300 cm −1 (Figure 4).Experimental ECD and VCD spectra of three C-1 epimeric pairs of 21 were compared in Figure 5, distinguishing the cis/trans configuration of the trimethoxyisochroman subunit.The ECD spectra of the C-1 epimers had significant differences in the 220-240 nm range, while minor differences appeared for the weak C-H deformation vibrations (1200-1300 cm −1 ) in the VCD spectra.Compared to the stereoisomers of 21, the atropodiastereomeric (aR,1S,3S,1′S,3′S)-22 and (aS,1S,3S,1′S,3′S)-22 possessed an additional chirality center at C-1′ with an ethoxycarbonyl substituent and both of them had cis relative configuration in the dimethoxyisochroman subunit and trans one in the trimethoxyisochroman.The ECD spectra of the (aR) and (aS) atropodiastereomers of 22 were quite similar, showing negative CEs above 210 nm and an intense positive one below it (Figure 6a).The differences in the ECD spectra in the relative intensities and shape could not be used to assign the axial chirality even with the aid of TDDFT-ECD calculations, which, however, reproduced the experimental ECD curves well.Compared to the stereoisomers of 21, the atropodiastereomeric (aR,1S,3S,1 ′ S,3 ′ S)-22 and (aS,1S,3S,1 ′ S,3 ′ S)-22 possessed an additional chirality center at C-1 ′ with an ethoxycarbonyl substituent and both of them had cis relative configuration in the dimethoxyisochroman subunit and trans one in the trimethoxyisochroman.The ECD spectra of the (aR) and (aS) atropodiastereomers of 22 were quite similar, showing negative CEs above 210 nm and an intense positive one below it (Figure 6a).The differences in the ECD spectra in the relative intensities and shape could not be used to assign the axial chirality even with the aid of TDDFT-ECD calculations, which, however, reproduced the experimental ECD curves well.
(aR) and (aS) atropodiastereomers of 22 were quite similar, showing negative CEs above 210 nm and an intense positive one below it (Figure 6a).The differences in the ECD spectra in the relative intensities and shape could not be used to assign the axial chirality even with the aid of TDDFT-ECD calculations, which, however, reproduced the experimenta ECD curves well.The experimental VCD spectra of the atropodiastereomeric (aR,1S,3S,1 ′ S,3 ′ S)-22 and (aS,1S,3S,1 ′ S,3 ′ S)-22 differing only in the axial chirality had near-mirror-image VCD transitions in the 1000-1500 cm −1 wavenumber range (Figure 6b).The VCD calculations gave good agreements with the experimental curves, which allowed the determination of the axial chirality.Due to the large similarity with the VCD spectra of the stereoisomers of 21, the axial chirality of (aR)-and (aS)-22 could have been deduced by simple comparison of the characteristic VCD transitions.
negative CEs above and positive ones below 210 nm.However, the broad negative transition of (aS,1R,3S,1′S,3′S)-22 (225 nm Δε = −27.82)was much more intense than the corresponding one of (aS,1S,3S,1′S,3′S)-22 (231 nm Δε = −7.84),and they had also different shapes and shoulders.These distinct differences can be used to assign the AC of the C-1 chirality centers in the C-1 epimers.The VCD spectra of the C-1 epimeric (aS,1R,3S,1′S,3′S)-22 and (aS,1S,3S,1′S,3′S)-22 showed the same signs for most of the CEs in the range of 1000-1500 cm −1 , reflecting their identical (aS) axial chirality, and VCD differences were even more subtle than those in the ECD spectra (Figure 7b).These differences consisted of three weak oppositely signed VCD transitions in the 1220-1290 cm −1 range, highlighted in Figure 7b, and the B3LYP/TZVP PCM/CHCl3 VCD spectrum of (aS,1S,3S,1′S,3′S)-22 reproduced the signs and shapes for one of them, which can be used to distinguish the C-1 epimers of 22 with VCD.
In some cases, the 1 H NMR signals of the diastereotopic 4-H a /4-H b and 4 ′ -H a /4 ′ -H b protons appeared separately, and their characteristic NOE correlations could be measured with aromatic or methoxy protons of the other isochroman residue, which could be used to determine the axial chirality in the knowledge of the AC of the central chirality elements (Figures S63, S70, S77, S84).As an example, the characteristic NOE correlations are shown for (aS,1S,3S,1 ′ S,3 ′ S)-22, suggesting (aS) axial chirality (Figure 8).In contrast to the VCD spectra, this approach could not be applied universally to assign the axial chirality.
The VCD spectra of the (aR) and (aS) atropisomers of 21-23 were compared (Figure 10), and it was found that regardless of the type of the C-1 ′ substitution (H, COOEt, or CH 2 COOEt) and AC of the central chirality elements, there are conserved characteristic VCD transitions, which reflect the different axial chirality of the biaryl axis.Four characteristic wavelength ranges are highlighted in Figure 10 but there are additional characteristic bands above 1400 cm −1 and below 1100 cm −1 .For example, two intense positive VCD couplets were identified, centered around 1350 cm −1 and 1100 cm −1 for the (aR) atropisomers of 21-23 (Figure 10a), which had opposite signs for the corresponding (aS) atropodiastereomers (Figure 10b).The analysis of the computed VCD transitions revealed that almost all the VCD bands had some contributions from different vibrational modes of the biaryl subunit, especially from carbon-carbon stretching vibrations.These contributions are responsible for the mirror-image VCD signals of the atropodiastereomers, while VCD bands reflecting central chirality elements had significant vibrational components from the aliphatic moieties.
sign for most of the CEs, including the most intense ones reflecting the axial chirality (Figure 9c).However, some distinct VCD transitions could be identified in C-H deformation vibration region with opposite CE for the pairs, which reflected the opposite configuration of the isochroman residues.The VCD spectra of the (aR) and (aS) atropisomers of 21-23 were compared (Figure 10), and it was found that regardless of the type of the C-1′ substitution (H, COOEt, or CH2COOEt) and AC of the central chirality elements, there are conserved characteristic VCD transitions, which reflect the different axial chirality of the biaryl axis.Four characteristic wavelength ranges are highlighted in Figure 10 but there are additional characteristic bands above 1400 cm −1 and below 1100 cm −1 .For example, two intense positive VCD couplets were identified, centered around 1350 cm −1 and 1100 cm −1 for the (aR) atropisomers of 21-23 (Figure 10a), which had opposite signs for the corresponding (aS) atropodiastereomers (Figure 10b).The analysis of the computed VCD transitions revealed that almost all the VCD bands had some contributions from different vibrational modes of the biaryl subunit, especially from carbon-carbon stretching vibrations.These contributions are responsible for the mirror-image VCD signals of the atropodiastereomers, while VCD bands reflecting central chirality elements had significant vibrational components from the aliphatic moieties.In order to test the effect of the C-1 aryl substituent, which may have an excitoncoupled ECD interaction with the substituted biphenyl chromophore and influence VCD spectrum as well, ECD and VCD spectra of the atropodiastereomeric (aR,3S,3 ′ S)-28 and (aS,3S,3 ′ S)-28 were analyzed (Figure 11).The experimental ECD spectra of the atropodiastereomeric (aR,3S,3 ′ S)-28 and (aS,3S,3 ′ S)-28b showed the same pattern with negative CEs at higher and a positive one at lower wavelength (Figure 11a), which confirmed that it is not the presence of the C-1 aryl group and a C-1 chirality center that is responsible for the near-identical ECD spectra of the atropodiastereomers.ECD spectra were characteristic of the C-3 and C-3 ′ chirality centers, which determined the preferred helicity of the condensed heteroring.In order to test the effect of the C-1 aryl substituent, which may have an excitoncoupled ECD interaction with the substituted biphenyl chromophore and influence VCD spectrum as well, ECD and VCD spectra of the atropodiastereomeric (aR,3S,3′S)-28 and (aS,3S,3′S)-28 were analyzed (Figure 11).The experimental ECD spectra of the atropodiastereomeric (aR,3S,3′S)-28 and (aS,3S,3′S)-28b showed the same pattern with negative CEs at higher and a positive one at lower wavelength (Figure 11a), which confirmed that it is not the presence of the C-1 aryl group and a C-1 chirality center that is responsible for the near-identical ECD spectra of the atropodiastereomers.ECD spectra were characteristic of the C-3 and C-3′ chirality centers, which determined the preferred helicity of the condensed heteroring.
The (aS) and (aR) atropodiastereomers of all the prepared axially chiral bis-isochromans showed anomalous ECD behavior, since their ECD spectra were not mirror-image curves and they did not reflect the chirality of the stereogenic biaryl axis.The near-identical ECD spectra of atropodiastereomeric (aR,3S,3′S)-28 and (aS,3S,3′S)-28 proved that 5,5′ biaryl linkage and the 6,7,8,7′,8′-pentamethoxy substitution pattern were responsible for the ECD discrepancy, which oriented the electric transition moments of the isochroman residues in a way that efficient exciton-coupled interaction was not possible.Thus, the ECD spectrum was governed by the central chirality elements, which is usually not the case in biaryls containing both central and axial chirality elements.
Interestingly, the experimental ECD spectra of the atropoisomeric penicisteckins A,B (2,3) and penicisteckins C,D (4,5), biaryl-type hetero-and homodimeric bis-isochroman natural products with 7,5′-and 7,7′-linkages differing only in the axial chirality, showed opposite CEs for the corresponding ECD transitions of the atropodiastereomers (Figure 11c).Similarly to 28, penicisteckins A-D (2-5) had a methylene group at C-1 and C-1′, but the different ECD behavior was attributed to the different biaryl linkage and aromatic substitution pattern, which enabled an enhanced interaction of the two isochroman moieties.The (aS) and (aR) atropodiastereomers of all the prepared axially chiral bis-isochromans showed anomalous ECD behavior, since their ECD spectra were not mirror-image curves and they did not reflect the chirality of the stereogenic biaryl axis.The near-identical ECD spectra of atropodiastereomeric (aR,3S,3 ′ S)-28 and (aS,3S,3 ′ S)-28 proved that 5,5 ′ biaryl linkage and the 6,7,8,7 ′ ,8 ′ -pentamethoxy substitution pattern were responsible for the ECD discrepancy, which oriented the electric transition moments of the isochroman residues in a way that efficient exciton-coupled interaction was not possible.Thus, the ECD spectrum was governed by the central chirality elements, which is usually not the case in biaryls containing both central and axial chirality elements.
Interestingly, the experimental ECD spectra of the atropoisomeric penicisteckins A,B (2,3) and penicisteckins C,D (4,5), biaryl-type hetero-and homodimeric bis-isochroman natural products with 7,5 ′ -and 7,7 ′ -linkages differing only in the axial chirality, showed opposite CEs for the corresponding ECD transitions of the atropodiastereomers (Figure 11c).Similarly to 28, penicisteckins A-D (2-5) had a methylene group at C-1 and C-1 ′ , but the different ECD behavior was attributed to the different biaryl linkage and aromatic substitution pattern, which enabled an enhanced interaction of the two isochroman moieties.
The VCD spectra of the atropodiastereomers (aR,3S,3 ′ S)-28 and (aS,3S,3 ′ S)-28 had oppositely signed CEs for the major transitions, and a simple comparison with those of the stereoisomers of 21-23 allowed the assignment of the axial chirality.The (aS,3S,3 ′ S)-28 stereoisomer had two intense negative VCD couplets centered at 1350 (negative CE at 1315 cm −1 , positive CE at 1362 cm −1 ) and 1100 cm −1 and (negative CE at 1084 cm −1 and a positive one at 1115 cm −1 ).The VCD spectra of the atropodiastereomers (aR,3S,3′S)-28 and (aS,3S,3′S)-28 had oppositely signed CEs for the major transitions, and a simple comparison with those of the stereoisomers of 21-23 allowed the assignment of the axial chirality.The (aS,3S,3′S)-28 stereoisomer had two intense negative VCD couplets centered at 1350 (negative CE at 1315 cm −1 , positive CE at 1362 cm −1 ) and 1100 cm −1 and (negative CE at 1084 cm −1 and a positive one at 1115 cm −1 ).

General Information
Chemicals were purchased puriss p.a. from commercial suppliers.Thin-layer chromatography (TLC) was performed on Silica gel 60 F254 (Merck) with visualization by UV light (254 nm) and immersing into aqueous solution of sulfuric acidic ammonium molybdate or 5% ethanolic phosphomolybdic acid solution followed by heating.Flash column chromatography was performed on Silica gel 60 (Merck 0.040-0.063mm).Melting points

General Information
Chemicals were purchased puriss p.a. from commercial suppliers.Thin-layer chromatography (TLC) was performed on Silica gel 60 F 254 (Merck) with visualization by UV light (254 nm) and immersing into aqueous solution of sulfuric acidic ammonium molybdate or 5% ethanolic phosphomolybdic acid solution followed by heating.Flash column chromatography was performed on Silica gel 60 (Merck 0.040-0.063mm).Melting points were determined on a Kofler hot-stage apparatus and were uncorrected.Anhydrous solvents were used for all the reactions and distilled solvents were used as eluent for flash chromatography.HPLC-grade solvents were used for chiral HPLC separations.Preparative chiral HPLC was performed by Agilent 1260 Infinity II apparatus using a Chiralpak IC column.The 1 H NMR (400 MHz) and 13 C NMR (100 MHz) spectra were recorded with a Bruker Avance I 400 MHz spectrometer at 298 K.Chemical shifts are referenced to Me 4 Si (0.00 ppm for 1 H) and to the residual solvent signals (CDCl 3 : 77.16 ppm for 13 C).Chemical shifts are reported as δ in ppm, and 1 J C,F , 2 J H,H and 3 J H,H coupling constants in Hz.IR spectra were recorded on a JASCO FT/IR-4100 spectrometer and absorption bands are presented as wavenumber in cm −1 .Optical rotations were measured at room temperature with a Perkin-Elmer 241 automatic polarimeter (c (g/100 mL)).ECD spectra were recorded on a J-810 spectropolarimeter.VCD measurements were performed on a BioTools ChiralIR-2X spectrometer at a resolution of 4 cm −1 under ambient temperature for 18 × 3000 scans, respectively.Samples were dissolved in CDCl 3 and the solutions were placed in a 100 µm BaF 2 cell.For spectroscopic measurements, spectroscopic grade solvents were used.Diffraction intensity data were collected at room temperature and the in case of (aS,1R,3R,1 ′ R,3 ′ R)-22 at low temperature (120 K) using a Bruker-D8 Venture diffractometer (Bruker AXS GmbH, Karlsruhe, Germany) equipped with INCOATEC IµS 3.0 (Incoatec GmbH, Geesthacht, Germany) dual (Cu and Mo) sealed tube microsources and a Photon II Charge-Integrating Pixel Array detector (Bruker AXS GmbH, Karlsruhe, Germany) using Mo Kα (λ = 0.71073 Å) radiation.Electrospray quadrupole time-of-flight HRMS measurements were performed with a MicroTOF-Q type QqTOF MS instrument equipped with an ESI source from Bruker (Bruker Daltoniks, Bremen, Germany).

Computational Section
Mixed torsional/low-frequency mode conformational searches were carried out by means of the Macromodel 10.8.011 software, using the Merck molecular force field (MMFF) with an implicit solvent model for CHCl 3 [32].All quantum chemical calculations were carried out with the Gaussian 09 software package [33,34].The B3LYP (VCD) and ωB97X [35] (ECD) functionals with the TZVP basis set and PCM solvent model for CHCl 3 (VCD) and MeCN (ECD) were used to reoptimize the initial MMFF geometries.TDDFT-ECD and -OR calculations were performed at the B3LYP/TZVP, BH&HLYP/TZVP, CAM-B3LYP/TZVP, and the PBE0/TZVP levels of theory with the PCM solvent model for MeCN.ECD spectra were generated as sums of Gaussians with 2100-3000 cm −1 widths at half-height, using dipole-velocity-computed rotational strength values [36].VCD calculations were performed at the B3LYP/TZVP PCM/CHCl 3 level, while the spectra were gained by applying a 8 cm −1 half-height width and scaled by a factor of 0.985.Boltzmann distributions were estimated from the B3LYP and ωB97X energies.The MOLEKEL 5.4 software package was used for visualization of the results [37].

X-ray Analysis
X-ray-quality crystals were grown by slow evaporation of the sample dissolved in a mixture of hexane and EtOH.A crystal well-looking in polarized light microscope was fixed under a microscope onto a Mitegen loop using high-density oil.Diffraction intensity data were collected at room temperature and in case of (aS,1R,3R,1 ′ R,3 ′ R)-22 at low temperature (120 K) using a Bruker-D8 Venture diffractometer (Bruker AXS GmbH, Karlsruhe, Germany) equipped with INCOATEC IµS 3.0 (Incoatec GmbH, Geesthacht, Germany) dual (Cu and Mo) sealed tube micro sources and a Photon II Charge-Integrating Pixel Array detector (Bruker AXS GmbH, Karlsruhe, Germany) using Mo Kα (λ = 0.71073 Å) radiation.The absolute configurations were assigned relative of the known configuration of C-3 and hence the applied radiation the Flack parameter is meaningless [38], but the assignment is unambiguous.Other spectroscopic methods (VCD, ECD) support the 100% enantiopurity of the samples.High multiplicity data collection and integration were performed using APEX4 (version 2021-4.0,Bruker AXS Inc., 2021, Madison, WI, USA) software.Data reduction and multi-scan absorption correction were performed using SAINT (version 8.40B, Bruker AXS Inc., 2019, Madison, USA).The structures were routinely solved using direct methods and refined on F 2 using the SHELXL program [39] incorporated into the APEX4 suite.Refinement was performed anisotropically for all non-hydrogen atoms.Hydrogen atoms were placed into geometric positions except for the hydrogen atoms of solvent ethanol molecules in the structure of (aS,1R,3R,1 ′ R,3 ′ R)-22.These atoms could be found on the difference electron density map and the respective O-H distances should be restrained.Multi-scan absorption correction had to be applied because of the irregular shape of the crystals especially in the case of (aS,1R,3R,3 ′ R)-21 (large crystals) and (aS,1R,3R,1 ′ R,3 ′ R)-22 (very small needle crystals).In latter case, RIGU command was used to regulate the refinement resulting in significant number of restrains.Further experimental details are shown in Table S1.The CIF file was manually edited using Publcif software [40], while graphics were prepared by using the Mercury program [41].The results for the X-ray diffraction structure determinations were good enough and acceptable according to the Checkcif functionality of the PLATON software (Utrecht University, Utrecht, The Netherlands) [42].Structural parameters such as bond length and angle data were in the expected range (Figure S269 and Table S2, Figure S270 and Table S3 as well as Figure S271 and Table S4 for (aR,1S,3S,3 ′ S)-21, (aS,1R,3R,3 ′ R)-21 and (aS,1R,3R,1 ′ R,3 ′ R)-22, respectively).The solid-state structures are stabilized by van der Waals interactions as well as by weak C-H••O and in case of (aS,1R,3R,1 ′ R,3 ′ R)-22 by strong O-H••O hydrogen bonds.As expected, (aR,1S,3S,3 ′ S)-21 and (aS,1R,3R,3 ′ R)-21 crystallized in unit cells of identical geometric parameters.The most interesting structure is (aS,1R,3R,1 ′ R,3 ′ R)-22 in which there were three molecules in the asymmetric unit together with two (slightly disordered) solvent ethanol molecules.There were only minor conformational differences among the molecules (Figure S272) and they have the same axial chirality.The supplementary crystallographic data can be obtained free of charge from the Cambridge Crystallographic Data Centre via http://www.ccdc.cam.ac.uk/data_request/cif (accessed on 28 August 2024), using reference deposition number 2249290 for (aR,1S,3S,3 ′ S)-21, 2249291 for (aS,1R,3R,3 ′ R)-21, and 2249292 for (aS,1R,3R,1 ′ R,3 ′ R)-22.

Conclusions
Stereoselective synthesis of heterodimeric 5,5 ′ -linked bis-isochromans, containing a stereogenic ortho-trisubstituted biaryl axis and up to four chirality centers, was achieved using a Suzuki-Miyaura biaryl coupling reaction of optically active isochroman and 1arylpropan-2-ol derivatives.Up to seven stereoisomers of the four target compounds differing in the C-1 and C-1 ′ substitution were prepared, which were used as model compounds with three isolated blocks of chirality to determine axial and central chirality elements parallel by OR, ECD, and VCD measurements and DFT calculations.Experimental VCD spectra of seven stereoisomers could be compared, which contained three chirality centers and a stereogenic biaryl axis in three isolated blocks of chirality.The effect of different C-1 and C-1 ′ substitution on the VCD spectra was also checked and characteristic VCD bands were identified, which reported the axial chirality regardless of different substitution pattern and configuration of the chirality centers.The stereochemical analysis was also supported by single-crystal X-ray analysis and NOE measurements.In contrast to related biaryl-type dimers such a penicisteckins A-D, we found that the ECD spectra and OR data of (aS) and (aR) atropodiastereomers were quite similar and did not reflect the opposite axial chirality.However, the atropodiastereomers showed consistently nearmirror-image VCD curves, allowing the determination of axial chirality with the aid of DFT calculation.The ECD spectra were dependent on the configuration of the chirality centers, which also governed the helicity of the heteroring in the isochroman subunits.Weak VCD transitions were identified in the C-H deformation vibration region, which could serve to distinguish stereoisomers with different central chirality elements.In the chiroptical analysis of our bis-isochromans, we demonstrated the complimentary nature of ECD, OR, and VCD methods to determine the parallel AC of central and axial chirality elements in three isolated blocks of chirality.
2-ol conjugate B, which diastereoselectively established a new C-1 ′ chirality center and allowed the variation of the C-1 substituent (Scheme 1).The key step of the scheme is the Suzuki-Miyaura biaryl cross-coupling reaction of cisor trans-5-iodoisochromans C with the pinacolatoboronate ester derivative (S)-8, which produced the ortho-trisubstituted stereogenic biaryl axis [C + (S)-8 → B].Chirality transfer from central to axial is expected to take place during formation of the biaryl axis.The boronate ester derivative (S)-8 and the 5-iodoisochromans C could be traced back to (S)-propylenoxide [(S)-11] [28] in two separate three-and four-step sequences.

Figure 4 .
Figure 4. Comparison of the experimental ECD and VCD spectra of stereoisomers of 21 differing in three or two central chirality centers.Figure 4. Comparison of the experimental ECD and VCD spectra of stereoisomers of 21 differing in three or two central chirality centers.

Figure 4 .Figure 5 .
Figure 4. Comparison of the experimental ECD and VCD spectra of stereoisomers of 21 differing in three or two central chirality centers.Figure 4. Comparison of the experimental ECD and VCD spectra of stereoisomers of 21 differing in three or two central chirality centers.

Figure 5 .
Figure 5.Comparison of the experimental ECD and VCD spectra of C-1 epimeric pairs of 21 (cis versus trans).

Figure 8 .
Figure8.Characteristic NOE correlations of (aS,1S,3S,1′S,3′S)-22, suggesting (1S,3S,1′S,3′S) configurations of the isochroman subunits and (aS) axial chirality as shown on the lowest-energy computed conformer.The red colored arrows shows the NOE correlations for determining of axial chirality, while blue purple ones for the central chirality of the two difference isochromans.

1 )Figure 10 .
Figure 10.Overlapped ten and nine VCD spectra of the (a) (aR) and (b) (aS) atropisomers of 21-23 differing in the AC of the central chirality elements and the C-1′ substitution.

Figure 10 .
Figure 10.Overlapped ten and nine VCD spectra of the (a) (aR) and (b) (aS) atropisomers of 21-23 differing in the AC of the central chirality elements and the C-1 ′ substitution.